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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2666968copy number variation130estd199human GRCh37 chr22: 45,135,251-45,137,530 , GRCh38.p12 chr22: 44,739,371-44,741,650 PRR5-ARHGAP8

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